Meckel syndrome, type 5

Any Meckel syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.

Also known as: MKS5, Meckel syndrome caused by mutation in RPGRIP1L, Meckel syndrome, type 5, RPGRIP1L Meckel syndrome, Meckel syndrome 5

37 clinical trials for this condition and its sub-types.